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Virtual Reality Mindfulness in Preoperative Anxious Patients

O

Ospedale Regionale di Mendrisio

Status

Enrolling

Conditions

Preoperative Period
Test Anxiety
Anxiety State

Treatments

Other: application for mindfulness
Device: Virtual Reality

Study type

Interventional

Funder types

Other

Identifiers

NCT05860192
APolito1

Details and patient eligibility

About

The goal of this interventional study is to reduce preoperative anxiety by Virtual Reality mindfulness.

Population: all adults, able to give their consent and scheduled for surgery with high preoperative anxiety defined by Amsterdam Preoperative Anxiety and Information Scale (APAIS) score > 10. The study will recruit 100 patients in one university teaching hospital.

The main question it aims to answer is: may mindfulness by Virtual Reality reduce preoperative anxiety in patients particularly anxious for the surgery? Participants will be asked to undergo to a single mindfulness virtual reality session before the surgery.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • adults able to give their consent, scheduled for elective surgery and with high preoperative anxiety defined by Amsterdam Preoperative Anxiety and Information Scale (APAIS) > 10

Exclusion criteria

  • Pregnancy
  • Epilepsy
  • Pacemaker wearers
  • Mental diseases
  • Alcohol or drug addiction
  • Severe hearing loss or blindness
  • Simultaneous participation to other studies

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Virtual Reality
Experimental group
Description:
Each patient undergoes to a virtual reality session of mindfullness. This lasts about 30 minutes.
Treatment:
Other: application for mindfulness
Device: Virtual Reality

Trial contacts and locations

1

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Central trial contact

Andrea Polito

Data sourced from clinicaltrials.gov

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